HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325363Generated: October 26, 2026
Water → Ethyl 2-[[(1,1-dimethylpropoxy)carbonyl]amino]-4-thiazoleacetate
https://huagongshe.com/reaction/325363
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Thiazoleacetic acid, 2-amino-, ethyl ester | HCID 104454 | — |
| Reactant | 2-Methylbutan-2-yl carbonochloridate | HCID 15051328 | — |
| Reactant | HCID 178470764 | HCID 178470764 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-[[(1,1-dimethylpropoxy)carbonyl]amino]-4-thiazoleacetate | HCID 19978738 | — |
Reaction Steps
To a solution of ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate, which can be represented as ethyl 2-(2-imino-2,3-dihydro-1,3-thiazol-4-yl)acetate, (14 g.) in a mixture of pyridine (40 g.) and methylene chloride (300 ml.) was gradually added diethyl ether solution of tert-pentyl chloroformate (70 ml.) containing 0.35 mole of tert-pentyl chloroformate over 10 minutes at -20° C. with stirring, and the mixture was stirred for 2 hours at the same temperature and further stirred for 0.5 hour at 0° C. After the reaction, the reaction mixture was poured into water (200 ml.), and then the organic layer was separated. The organic layer was washed with 2 N hydrochloric acid, water, 5% sodium bicarbonate aqueous solution and water in turn and then dried over magnesium sulfate. The solvent was distilled off from the organic layer to give dark brown oil of ethyl 2-(2-tert-pentyloxycarbonylamino-1,3-thiazol-4-yl)acetate, which can be represented as ethyl 2-(2-tert-pentyloxycarbonylimino-2,3-dihydro-1,3-thiazol-4-yl)acetate, (12 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04440766 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-5c97246ed8f147dea1ac3fc95a6bb469 |
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| Source note | uspto-grants-1984_04 |
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